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Results for the Protein: NP_001139281
224831241

myosin-14 isoform 3 [Homo sapiens]

Known Diseases associated with this Protein:
  DEAFNESS, AUTOSOMAL DOMINANT 4
  PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
6
3
6
3
0
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

 Clicking a check box will display or hide the correlated domain.

 To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic.



Default View:

COG5022 - COG5022
Myosin_N - pfam02736
MYSc_type_IX - cd01385
MYSc - smart00242
MYSc_type_VIII - cd01383
MYSc_type_II - cd01377
MYSc_type_VI - cd01382
MYSc_type_XI - cd01384
MYSc_type_XV - cd01387
MYSc_type_III - cd01379
MYSc_type_XVIII - cd01386
MYSc_type_V - cd01380
MYSc - cd00124
MYSc_type_VII - cd01381
Myosin_head - pfam00063
MYSc_type_I - cd01378
Motor_domain - cd01363
IQ - smart00015
IQ - pfam00612
Myosin_tail_1 - pfam01576




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
MYSc_type_IXcd013852.5e-7899844
MYSc_type_VIIIcd013831.8e-150100840
MYSc_type_IIcd01377101840
MYSc_type_VIcd013821.8e-86102843
MYSc_type_XIcd013841.8e-190105845
MYSc_type_XVcd013877e-146105840
MYSccd001245.9e-277106840
MYSc_type_VIIcd013811.4e-176106840
MYSc_type_Vcd013806.4e-208106840
MYSc_type_XVIIIcd013869.5e-36106840
MYSc_type_IIIcd013793.2e-75106863
MYSc_type_Icd013784.2e-177108840
Motor_domaincd013632.2e-96141739
COG5022COG50227.1e-297351639
Myosin_Npfam027361.4e-065395
Myosin_headpfam00063107829
IQpfam006120.0002845865
Myosin_tail_1pfam015761.9e-18111311988
MYScsmart00242100841
IQsmart000151.8e-05843865

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs11669191 Polymorphismp.ALA1250GLUN/A
dbSNPrs75915336 Polymorphismp.GLY681ARGN/A
dbSNPrs34498817 Polymorphismp.PRO342ALAN/A
OMIM608568.0006 Diseasep.ARG941LEUPERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
OMIM608568.0003 Diseasep.ARG726SERDEAFNESS, AUTOSOMAL DOMINANT 4
OMIM608568.0004 Diseasep.GLY376CYSDEAFNESS, AUTOSOMAL DOMINANT 4
OMIM608568.0002 Diseasep.LEU976PHEDEAFNESS, AUTOSOMAL DOMINANT 4
OMIM608568.0005 Diseasep.SER120LEUDEAFNESS, AUTOSOMAL DOMINANT 4
OMIM608568.0001 Diseasep.SER7TERDEAFNESS, AUTOSOMAL DOMINANT 4



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